No evidence for conspecific recruitment for cooperative hunting in lionfish Pterois miles

Lionfish are common piscivores in the Indo-Pacific and invasive in the Caribbean. A fin flaring pattern, involving a rapid undulation of the caudal fin and sequential turning of both pectoral fins, was described in zebra lionfish as a signal to initiate cooperative hunting, and it was hypothesized that such hunting tactics may also exist in other lionfish species and contribute to their successful invasion in the Caribbean. Here, we investigated one of those invasive species, Pterois miles , in its natural range in the Red Sea. We did not observe evidence for cooperative hunting in the field. We complemented field observations with a laboratory experiment aimed at inducing subjects to recruit partners for cooperative hunts, exposing subjects to inaccessible prey in transparent housing as well as to a potential partner. We regularly observed the fin flaring pattern, but importantly, it was not directed at the partner. Thus, rather than being a signal, the fin flaring movement pattern seems to be a swimming mode in a confined environment. Furthermore, the two lionfish did not aggregate at the prey housing, reinforcing the field results that this species in the Red Sea does not depend on cooperation to hunt fish.

Cool your jets: biological jet propulsion in marine invertebrates

ABSTRACT Pulsatile jet propulsion is a common swimming mode used by a diverse array of aquatic taxa from chordates to cnidarians. This mode of locomotion has interested both biologists and engineers for over a century. A central issue to understanding the important features of jet-propelling animals is to determine how the animal interacts with the surrounding fluid. Much of our knowledge of aquatic jet propulsion has come from simple theoretical approximations of both propulsive and resistive forces. Although these models and basic kinematic measurements have contributed greatly, they alone cannot provide the detailed information needed for a comprehensive, mechanistic overview of how jet propulsion functions across multiple taxa, size scales and through development. However, more recently, novel experimental tools such as high-speed 2D and 3D particle image velocimetry have permitted detailed quantification of the fluid dynamics of aquatic jet propulsion. Here, we provide a comparative analysis of a variety of parameters such as efficiency, kinematics and jet parameters, and review how they can aid our understanding of the principles of aquatic jet propulsion. Research on disparate taxa allows comparison of the similarities and differences between them and contributes to a more robust understanding of aquatic jet propulsion.

The effect of locomotion mode on body shape evolution in teleost fishes

Teleost fishes vary in their reliance on median and paired fins (MPF) or undulation of the body (BCF) to generate thrust during straight-line, steady swimming. Previous work indicates that swimming mode is associated with different body shapes, though this has never been empirically demonstrated across the diversity of fishes. As the body does not play as active a mechanical role in steady swimming by MPF swimmers, this may relax constraints and spur higher rates of body shape diversification. We test these predictions by measuring the impact of the dominant steady swimming mode on the evolution of body shape across 2,295 marine teleost fishes. Aligning with historical expectations, BCF swimmers exhibit a more elongate, slender body shape, while MPF propulsion is associated with deeper and wider body shapes. However, in contrast to expectations, we find that BCF propulsion is associated with higher morphological diversity and greater variance around trait optima. This surprising result is consistent with the interpretation that stronger functional trade-offs stimulate phenotypic evolution, rather than constrain it.

Optimum Curvature Characteristics of Body/Caudal Fin Locomotion

Fish propelled by body and/or caudal fin (BCF) locomotion can achieve high-efficiency and high-speed swimming performance, by changing their body motion to interact with external fluids. This flexural body motion can be prescribed through its curvature profile. This work indicates that when the fish swims with high efficiency, the curvature amplitude reaches a maximum at the caudal peduncle. In the case of high-speed swimming, the curvature amplitude shows three maxima on the entire body length. It is also demonstrated that, when the Reynolds number is in the range of 104–106, the swimming speed, stride length, and Cost of Transport (COT) are all positively correlated with the tail-beat frequency. A sensitivity analysis of curvature amplitude explains which locations change the most when the fish switches from the high-efficiency swimming mode to the high-speed swimming mode. The comparison among three kinds of BCF fish shows that the optimal swimming performance of thunniform fish is almost the same as that of carangiform fish, while it is better not to neglect the reaction force acting on an anguilliform fish. This study provides a reference for curvature control of bionic fish in a future time.

Rethinking swimming performance tests for bottom-dwelling fish: the case of European glass eel (Anguilla anguilla)

Systematic experiments on European eel (Anguilla anguilla) in their juvenile, early life stage (glass eel), were conducted to provide new insights on the fish swimming performance and propose a framework of analysis to design swimming-performance experiments for bottom-dwelling fish. In particular, we coupled experimental and computational fluid dynamics techniques to: (i) accommodate glass eel burst-and-coast swimming mode and estimate the active swimming time (tac), not considering coast and drift periods, (ii) estimate near-bottom velocities (Ub) experienced by the fish, rather than using bulk averages (U), (iii) investigate water temperature (T) influence on swimming ability, and (iv) identify a functional relation between Ub, tac and T. Results showed that burst-and-coast swimming mode was increasingly adopted by glass eel, especially when U was higher than 0.3 ms-1. Using U rather than Ub led to an overestimation of the fish swimming performance from 18 to 32%, on average. Under the range of temperatures analyzed (from 8 to 18 °C), tac was strongly influenced and positively related to T. As a final result, we propose a general formula to link near-bottom velocity, water temperature and active swimming time which can be useful in ecological engineering applications and reads as $${\rm{U}}_{\rm{b}}=0.174\cdot \left({{\rm{t}}_{\rm{ac}}}^{-0.36}\cdot {\rm{T}}^{0.77}\right)$$ U b = 0.174 · t ac - 0.36 · T 0.77 .

Distinct chemotactic behavior in the original Escherichia coli K-12 depending on forward-and-backward swimming, not on run-tumble movements

Most motile bacteria are propelled by rigid, helical, flagellar filaments and display distinct swimming patterns to explore their favorable environments. Escherichia coli cells have a reversible rotary motor at the base of each filament. They exhibit a run-tumble swimming pattern, driven by switching of the rotational direction, which causes polymorphic flagellar transformation. Here we report a novel swimming mode in E. coli ATCC10798, which is one of the original K-12 clones. High-speed tracking of single ATCC10798 cells showed forward and backward swimming with an average turning angle of 150°. The flagellar helicity remained right-handed with a 1.3 μm pitch and 0.14 μm helix radius, which is consistent with the feature of a curly type, regardless of motor switching; the flagella of ATCC10798 did not show polymorphic transformation. The torque and rotational switching of the motor was almost identical to the E. coli W3110 strain, which is a derivative of K-12 and a wild-type for chemotaxis. The single point mutation of N87K in FliC, one of the filament subunits, is critical to the change in flagellar morphology and swimming pattern, and lack of flagellar polymorphism. E. coli cells expressing FliC(N87K) sensed ascending a chemotactic gradient in liquid but did not spread on a semi-solid surface. Based on these results, we concluded that a flagellar polymorphism is essential for spreading in structured environments.

Swimming behavior and performance of the marsh rat Holochilus vulpinus (Brants, 1827) (Cricetidae, Sigmodontinae)

Semiaquatic habits evolved in several Sigmodontinae rodent species, but this issue remains poorly studied. The marsh rat Holochilus vulpinus (Brants, 1827) has been associated with palustrine wetland environments and exhibits several morphological traits related to the semiaquatic habit. However, its swimming behavior and the way its morphological specializations contribute to it have not been evaluated so far in this species. This note focuses on describing and quantifying the swimming behavior and swimming performance of H. vulpinus. In order to address these issues, five individuals of H. vulpinus, four adults and one subadult, were filmed while swimming and their performance was quantified. The obtained results indicate that the swimming mode is bipedal paddling, alternating the stroke of the hind feet. The quantitative indicators also qualify H. vulpinus as a good swimmer compared to other terrestrial and semiaquatic mammals.

Swimming and defence: competing needs across ontogeny in armoured fishes (Agonidae)

Biological armours are potent model systems for understanding the complex series of competing demands on protective exoskeletons; after all, armoured organisms are the product of millions of years of refined engineering under the harshest conditions. Fishes are no strangers to armour, with various types of armour plating common to the 400–500 Myr of evolution in both jawed and jawless fishes. Here, we focus on the poachers (Agonidae), a family of armoured fishes native to temperate waters of the Pacific rim. We examined armour morphology, body stiffness and swimming performance in the northern spearnose poacher ( Agonopsis vulsa ) over ontogeny. As juveniles, these fishes make frequent nocturnal forays into the water column in search of food, while heavily armoured adults are bound to the benthos. Most armour dimensions and density increase with body length, as does body stiffness. Juvenile poachers have enlarged spines on their armour whereas adults invest more mineral in armour plate bases. Adults are stiffer and accelerate faster than juveniles with an anguilliform swimming mode. Subadults more closely approximate adults more than smaller juveniles, with regards to both swimming and armour mechanics. Poacher armour serves multiple functions over ontogeny, from facilitating locomotion, slowing sinking and providing defence.